Beth Keena

1.1k total citations
13 papers, 221 citations indexed

About

Beth Keena is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Beth Keena has authored 13 papers receiving a total of 221 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 6 papers in Genetics and 2 papers in Surgery. Recurrent topics in Beth Keena's work include Genetics and Neurodevelopmental Disorders (2 papers), Cleft Lip and Palate Research (2 papers) and Congenital Diaphragmatic Hernia Studies (2 papers). Beth Keena is often cited by papers focused on Genetics and Neurodevelopmental Disorders (2 papers), Cleft Lip and Palate Research (2 papers) and Congenital Diaphragmatic Hernia Studies (2 papers). Beth Keena collaborates with scholars based in United States, Canada and Italy. Beth Keena's co-authors include Judith G. Hall, David R. Witt, Judith Allanson, Elaine H. Zackai, John M. Opitz, James F. Reynolds, J. Bamforth, Bernard N. Chodirker, Jan M. Friedman and Jane Evans and has published in prestigious journals such as Pediatric Research, Epilepsy Research and American Journal of Medical Genetics.

In The Last Decade

Beth Keena

12 papers receiving 212 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Beth Keena United States 7 106 90 54 44 36 13 221
Barbara Sibbles Netherlands 9 121 1.1× 70 0.8× 70 1.3× 28 0.6× 28 0.8× 12 283
Federica Tamburrino Italy 9 102 1.0× 80 0.9× 15 0.3× 50 1.1× 13 0.4× 16 174
J M Cantú Mexico 10 72 0.7× 93 1.0× 45 0.8× 13 0.3× 17 0.5× 17 220
Neda Zadeh United States 7 152 1.4× 141 1.6× 25 0.5× 20 0.5× 28 0.8× 12 253
Márta Czakó Hungary 11 112 1.1× 141 1.6× 20 0.4× 7 0.2× 30 0.8× 40 245
Sigrun Fuchs Germany 9 204 1.9× 186 2.1× 17 0.3× 7 0.2× 61 1.7× 15 315
Selma A. Myhre United States 9 120 1.1× 148 1.6× 81 1.5× 6 0.1× 51 1.4× 11 310
Isabel Cordeiro Portugal 7 146 1.4× 162 1.8× 22 0.4× 7 0.2× 51 1.4× 14 296
Jean‐Pierre Fryns Belgium 9 160 1.5× 113 1.3× 64 1.2× 25 0.6× 57 1.6× 15 270
Stefano Petrocchi Italy 8 84 0.8× 129 1.4× 31 0.6× 22 0.5× 16 0.4× 15 236

Countries citing papers authored by Beth Keena

Since Specialization
Citations

This map shows the geographic impact of Beth Keena's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Beth Keena with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Beth Keena more than expected).

Fields of papers citing papers by Beth Keena

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Beth Keena. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Beth Keena. The network helps show where Beth Keena may publish in the future.

Co-authorship network of co-authors of Beth Keena

This figure shows the co-authorship network connecting the top 25 collaborators of Beth Keena. A scholar is included among the top collaborators of Beth Keena based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Beth Keena. Beth Keena is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

13 of 13 papers shown
1.
Campbell, Ian M., et al.. (2022). The experience of one pediatric geneticist with telemedicine‐based clinical diagnosis. American Journal of Medical Genetics Part A. 188(12). 3416–3422. 2 indexed citations
2.
Matalon, Dena R., David A. Stevenson, Elizabeth Bhoj, et al.. (2021). Congenital polyvalvular disease expands the cardiac phenotype of the RASopathies. American Journal of Medical Genetics Part A. 185(5). 1486–1493. 5 indexed citations
3.
Cohen, Jennifer L., Samantha A. Schrier Vergano, Alanna Strong, et al.. (2020). EP300‐related Rubinstein–Taybi syndrome: Highlighted rare phenotypic findings and a genotype–phenotype meta‐analysis of 74 patients. American Journal of Medical Genetics Part A. 182(12). 2926–2938. 18 indexed citations
4.
Rabin, Rachel, Yoel Hirsch, David A. Zeevi, et al.. (2019). Study of carrier frequency of Warsaw breakage syndrome in the Ashkenazi Jewish population and presentation of two cases. American Journal of Medical Genetics Part A. 179(10). 2144–2151. 13 indexed citations
5.
Murali, Chaya N., Beth Keena, & Elaine H. Zackai. (2018). Robinow syndrome: a diagnosis at the fingertips. Clinical Dysmorphology. 27(4). 135–137. 4 indexed citations
6.
Romasko, Edward J., Elizabeth T. DeChene, Jorune Balciuniene, et al.. (2018). PCDH19-related epilepsy in a male with Klinefelter syndrome: Additional evidence supporting PCDH19 cellular interference disease mechanism. Epilepsy Research. 145. 89–92. 17 indexed citations
7.
Bedeschi, Maria Francesca, Giuseppe Marangi, Mariarosaria Calvello, et al.. (2017). Impairment of different protein domains causes variable clinical presentation within Pitt-Hopkins syndrome and suggests intragenic molecular syndromology of TCF4. European Journal of Medical Genetics. 60(11). 565–571. 19 indexed citations
8.
Bamforth, J., Claire O. Leonard, Bernard N. Chodirker, et al.. (1989). Congenital diaphragmatic hernia, coarse facies, and acral hypoplasia: Fryns syndrome. American Journal of Medical Genetics. 32(1). 93–99. 53 indexed citations
9.
Sadovnick, A. Dessa, Patricia A. Baird, Judith G. Hall, et al.. (1987). Use of genetic counselling services for neural tube defects. American Journal of Medical Genetics. 26(4). 811–818. 6 indexed citations
10.
Pantzar, Tapio, et al.. (1987). FRYNS SYNDROME: FURTHER DELINEATION AND ANTENATAL DIAGNOSIS. Pediatric Research. 21(4). 224A–224A.
11.
Witt, David R., Beth Keena, Judith G. Hall, & Judith Allanson. (1986). Growth curves for height in Noonan syndrome. Clinical Genetics. 30(3). 150–153. 77 indexed citations
12.
Keena, Beth, A. Dessa Sadovnick, Patricia A. Baird, et al.. (1986). Risks to sibs of probands with neural tube defects: Data for clinic populations in British Columbia. American Journal of Medical Genetics. 25(3). 563–573. 6 indexed citations
13.
Sadovnick, A. Dessa, Beth Keena, Patricia A. Baird, & Judith G. Hall. (1986). Fetal mortality in sibships of cases with neural tube defects. Clinical Genetics. 29(5). 409–412. 1 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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